PDGF, TGF-β, and FGF signaling is important for differentiation and growth of mesenchymal stem cells (MSCs):: transcriptional profiling can identify markers and signaling pathways important in differentiation of MSCs into adipogenic, chondrogenic, and osteogenic lineages

被引:469
作者
Ng, Felicia [1 ]
Boucher, Shayne [2 ]
Koh, Susie [1 ]
Sastry, Konduru S. R. [1 ]
Chase, Lucas [2 ]
Lakshmipathy, Uma [2 ]
Choong, Cleo [3 ]
Yang, Zheng [4 ]
Vemuri, Mohan C. [2 ]
Rao, Mahendra S. [2 ]
Tanavde, Vivek [1 ]
机构
[1] ASTAR, Bioinformat Inst, Genome & Gene Express Anal Grp, Singapore 138671, Singapore
[2] Invitrogen Corp, Stem Cells & Regenerat Med, Carlsbad, CA USA
[3] Singapore Stem Cell Consortium, Lab Stem Cell Biol, Singapore, Singapore
[4] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Orthopaed Surg, Tissue Engn Program, Singapore, Singapore
关键词
D O I
10.1182/blood-2007-07-103697
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We compared the transcriptomes of marrow-derived mesenchymal stem cells (MSCs) with differentiated adipocytes, osteocytes, and chondrocytes derived from these MSCs. Using global gene-expression profiling arrays to detect RNA transcripts, we have identified markers that are specific for MSCs and their differentiated progeny. Further, we have also identified pathways that MSCs use to differentiate into adipogenic, chondrogenic, and osteogenic lineages. We identified activin-mediated transforming growth factor (TGF)-beta signaling, platelet-derived growth factor (PDGF) signaling and fibroblast growth factor (FGF) signaling as the key pathways involved in MSC differentiation. The differentiation of MSCs into these lineages is affected when these pathways are perturbed by inhibitors of cell surface receptor function. Since growth and differentiation are tightly linked processes, we also examined the importance of these 3 pathways in MSC growth. These 3 pathways were necessary and sufficient for MSC growth. Inhibiting any of these pathways slowed MSC growth, whereas a combination of TGF-beta, PDGF, and beta-FGF was sufficient to grow MSCs in a serum-free medium up to 5 passages. Thus, this study illustrates it is possible to predict signaling pathways active in cellular differentiation and growth using microarray data and experimentally verify these predictions.
引用
收藏
页码:295 / 307
页数:13
相关论文
共 58 条
[1]   Plasticity of human stem cells in the fetal sheep model of human stem cell transplantation [J].
Almeida-Porada, G ;
Porada, C ;
Zanjani, ED .
INTERNATIONAL JOURNAL OF HEMATOLOGY, 2004, 79 (01) :1-6
[2]   Adult mesenchymal stem cells: characterization, differentiation, and application in cell and gene therapy [J].
Baksh, D ;
Song, L ;
Tuan, RS .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2004, 8 (03) :301-316
[3]   Subcellular distribution and mitogenic effect of basic fibroblast growth factor in mesenchymal uncommitted stem cells [J].
Benavente, CA ;
Sierralta, WD ;
Conget, PA ;
Minguell, JJ .
GROWTH FACTORS, 2003, 21 (02) :87-94
[4]  
Beyer Nardi N, 2006, HANDB EXP PHARM, V174, P249
[5]   Critical parameters for the isolation of mesenchymal stem cells from umbilical cord blood [J].
Bieback, K ;
Kern, S ;
Klüter, H ;
Eichler, H .
STEM CELLS, 2004, 22 (04) :625-634
[6]   Fibroblast growth factors 2, 4, and 8 exert both negative and positive effects on limb, frontonasal, and mandibular chondrogenesis via MEK-ERK activation [J].
Bobick, Brent E. ;
Thornhill, Tasha M. ;
Kulyk, William M. .
JOURNAL OF CELLULAR PHYSIOLOGY, 2007, 211 (01) :233-243
[7]   Mesenchymal stem cells: building blocks for molecular medicine in the 21st century [J].
Caplan, AI ;
Bruder, SP .
TRENDS IN MOLECULAR MEDICINE, 2001, 7 (06) :259-264
[8]   The role of mesenchymal stem cells in haemopoiesis [J].
Dazzi, Francesco ;
Ramasamy, Rajesh ;
Glennie, Sarah ;
Jones, Simon P. ;
Roberts, Irene .
BLOOD REVIEWS, 2006, 20 (03) :161-171
[9]   Skeletal muscle repair by adult human mesenchymal stem cells from synovial membrane [J].
De Bari, C ;
Dell'Accio, F ;
Vandenabeele, F ;
Vermeesch, JR ;
Raymackcrs, JM ;
Luyten, FP .
JOURNAL OF CELL BIOLOGY, 2003, 160 (06) :909-918
[10]  
De Bari C, 2001, ARTHRITIS RHEUM-US, V44, P1928, DOI 10.1002/1529-0131(200108)44:8<1928::AID-ART331>3.0.CO